@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP168672.RAAaqVkBWxt779hgrUAYN0MlK9lQdvDOT4fLiZaZs4V90> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP168672.RAAaqVkBWxt779hgrUAYN0MlK9lQdvDOT4fLiZaZs4V90130_head {
  this: np:hasAssertion dgn-np:NP168672.RAAaqVkBWxt779hgrUAYN0MlK9lQdvDOT4fLiZaZs4V90130_assertion;
    np:hasProvenance dgn-np:NP168672.RAAaqVkBWxt779hgrUAYN0MlK9lQdvDOT4fLiZaZs4V90130_provenance;
    np:hasPublicationInfo dgn-np:NP168672.RAAaqVkBWxt779hgrUAYN0MlK9lQdvDOT4fLiZaZs4V90130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP168672.RAAaqVkBWxt779hgrUAYN0MlK9lQdvDOT4fLiZaZs4V90130_assertion a np:Assertion .
  
  dgn-np:NP168672.RAAaqVkBWxt779hgrUAYN0MlK9lQdvDOT4fLiZaZs4V90130_provenance a np:Provenance .
  
  dgn-np:NP168672.RAAaqVkBWxt779hgrUAYN0MlK9lQdvDOT4fLiZaZs4V90130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP168672.RAAaqVkBWxt779hgrUAYN0MlK9lQdvDOT4fLiZaZs4V90130_assertion {
  miriam-gene:57045 a ncit:C16612 .
  
  lld:C0700095 a ncit:C7057 .
  
  dgn-gda:DGN6ade6aeeffc357daa0de35456f543ce2 sio:SIO_000628 miriam-gene:57045, lld:C0700095;
    a sio:SIO_001121 .
}

dgn-np:NP168672.RAAaqVkBWxt779hgrUAYN0MlK9lQdvDOT4fLiZaZs4V90130_provenance {
  dgn-np:NP168672.RAAaqVkBWxt779hgrUAYN0MlK9lQdvDOT4fLiZaZs4V90130_assertion dcterms:description
      "[Loss of heterozygosity of several specific genomic regions is frequently observed in neuroblastoma tumors and cell lines, but homozygous deletion (HD) is rare, and no neuroblastoma tumor suppressor gene (TSG) has yet been identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:11212268;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP168672.RAAaqVkBWxt779hgrUAYN0MlK9lQdvDOT4fLiZaZs4V90130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:31+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}